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Watching DNA polymerase η make a phosphodiester bond
Native human DNA polymerase η, DNA and dATP were crystallized at pH 6.0 without Mg(2+). The polymerization reaction was initiated by exposing crystals to 1 mM Mg(2+) at pH 7.0, and stopped at various time points by freezing at 77 K for crystallographic analysis. The substrates and two Mg(2+) are ali...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397672/ https://www.ncbi.nlm.nih.gov/pubmed/22785315 http://dx.doi.org/10.1038/nature11181 |
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author | Nakamura, Teruya Zhao, Ye Yamagata, Yuriko Hua, Yue-jin Yang, Wei |
author_facet | Nakamura, Teruya Zhao, Ye Yamagata, Yuriko Hua, Yue-jin Yang, Wei |
author_sort | Nakamura, Teruya |
collection | PubMed |
description | Native human DNA polymerase η, DNA and dATP were crystallized at pH 6.0 without Mg(2+). The polymerization reaction was initiated by exposing crystals to 1 mM Mg(2+) at pH 7.0, and stopped at various time points by freezing at 77 K for crystallographic analysis. The substrates and two Mg(2+) are aligned for reaction within 40 seconds, but the new bond begins to form at 80 seconds. Structures at reaction times from 80s to 300s reveal a mixture of decreasing substrate and increasing product of the nucleotidyl-transfer reaction. In sequence, the nucleophile 3′-OH is deprotonated, the deoxyribose at the primer end converts from C2′-endo to C3′-endo to avoid steric clashes, and the nucleophile and the α-phosphate of dATP approach each other to form the new bond. A third Mg(2+) ion, which arrives with the new bond and stabilizes the intermediate state, may be an unappreciated feature of the two-metal-ion mechanism. |
format | Online Article Text |
id | pubmed-3397672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-33976722013-01-12 Watching DNA polymerase η make a phosphodiester bond Nakamura, Teruya Zhao, Ye Yamagata, Yuriko Hua, Yue-jin Yang, Wei Nature Article Native human DNA polymerase η, DNA and dATP were crystallized at pH 6.0 without Mg(2+). The polymerization reaction was initiated by exposing crystals to 1 mM Mg(2+) at pH 7.0, and stopped at various time points by freezing at 77 K for crystallographic analysis. The substrates and two Mg(2+) are aligned for reaction within 40 seconds, but the new bond begins to form at 80 seconds. Structures at reaction times from 80s to 300s reveal a mixture of decreasing substrate and increasing product of the nucleotidyl-transfer reaction. In sequence, the nucleophile 3′-OH is deprotonated, the deoxyribose at the primer end converts from C2′-endo to C3′-endo to avoid steric clashes, and the nucleophile and the α-phosphate of dATP approach each other to form the new bond. A third Mg(2+) ion, which arrives with the new bond and stabilizes the intermediate state, may be an unappreciated feature of the two-metal-ion mechanism. 2012-07-11 /pmc/articles/PMC3397672/ /pubmed/22785315 http://dx.doi.org/10.1038/nature11181 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Nakamura, Teruya Zhao, Ye Yamagata, Yuriko Hua, Yue-jin Yang, Wei Watching DNA polymerase η make a phosphodiester bond |
title | Watching DNA polymerase η make a phosphodiester bond |
title_full | Watching DNA polymerase η make a phosphodiester bond |
title_fullStr | Watching DNA polymerase η make a phosphodiester bond |
title_full_unstemmed | Watching DNA polymerase η make a phosphodiester bond |
title_short | Watching DNA polymerase η make a phosphodiester bond |
title_sort | watching dna polymerase η make a phosphodiester bond |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397672/ https://www.ncbi.nlm.nih.gov/pubmed/22785315 http://dx.doi.org/10.1038/nature11181 |
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